Polydactyly-myopia syndrome

Polydactyly-myopia syndrome is an exceedingly rare autosomal dominant developmental anomaly reported in 1986 in nine individuals among four generations of the same family. The syndrome is characterized clinically by four-limb postaxial polydactyly and progressive myopia. There have been no further descriptions in the literature since 1986.

Also known as: Czeizel-Brooser syndrome, polydactyly-myopia syndrome, Czeizel Brooser syndrome, PMS, polydactyly myopia syndrome, polydactyly, postaxial, with progressive myopia, postaxial polydactyly with progressive myopia, postaxial polydactyly-progressive myopia syndrome

2 clinical trials for this condition and its sub-types, 2 tagged with Polydactyly-myopia syndrome itself.